3AGV

Crystal structure of a human IgG-aptamer complex

Summary for 3AGV

• Entry DOI: 10.2210/pdb3agv/pdb
• Descriptor: Ig gamma-1 chain C region, 5'-R(*GP*GP*AP*GP*GP*(UFT)P*GP*(CFZ)P*(UFT)P*(CFZ)P*(CFZ)P*GP*AP*AP*A*GP*GP*AP*AP*(CFZ)P*(UFT)P*(CFZ)P*(CFZ)P*A)-3', alpha-D-galactopyranose-(1-4)-2-acetamido-2-deoxy-alpha-D-glucopyranose-(1-2)-alpha-D-mannopyranose-(1-6)-alpha-D-mannopyranose, ... (6 entities in total)
• Functional Keywords: igg, rna aptamer, immune system-rna complex, immune system/rna
• Biological source: Homo sapiens (human)
• Cellular location: Secreted: P01857
• Total number of polymer chains: 4
• Total formula weight: 65623.40

Authors

Nomura, Y.,Sugiyama, S.,Sakamoto, T.,Miyakawa, S.,Adachi, H.,Takano, K.,Murakami, S.,Inoue, T.,Mori, Y.,Nakamura, Y.,Matsumura, H. (deposition date: 2010-04-08, release date: 2010-11-10, Last modification date: 2024-11-20)

Primary citation

Nomura, Y.,Sugiyama, S.,Sakamoto, T.,Miyakawa, S.,Adachi, H.,Takano, K.,Murakami, S.,Inoue, T.,Mori, Y.,Nakamura, Y.,Matsumura, H.
Conformational plasticity of RNA for target recognition as revealed by the 2.15 A crystal structure of a human IgG-aptamer complex
Nucleic Acids Res., 38:7822-7829, 2010

PubMed Abstract: Aptamers are short single-stranded nucleic acids with high affinity to target molecules and are applicable to therapeutics and diagnostics. Regardless of an increasing number of reported aptamers, the structural basis of the interaction of RNA aptamer with proteins is poorly understood. Here, we determined the 2.15 Å crystal structure of the Fc fragment of human IgG1 (hFc1) complexed with an anti-Fc RNA aptamer. The aptamer adopts a characteristic structure fit to hFc1 that is stabilized by a calcium ion, and the binding activity of the aptamer can be controlled many times by calcium chelation and addition. Importantly, the aptamer-hFc1 interaction involves mainly van der Waals contacts and hydrogen bonds rather than electrostatic forces, in contrast to other known aptamer-protein complexes. Moreover, the aptamer-hFc1 interaction involves human IgG-specific amino acids, rendering the aptamer specific to human IgGs, and not crossreactive to other species IgGs. Hence, the aptamer is a potent alternative for protein A affinity purification of Fc-fusion proteins and therapeutic antibodies. These results demonstrate, from a structural viewpoint, that conformational plasticity and selectivity of an RNA aptamer is achieved by multiple interactions other than electrostatic forces, which is applicable to many protein targets of low or no affinity to nucleic acids.

PubMed: 20675355
DOI: 10.1093/nar/gkq615

Experimental method

X-RAY DIFFRACTION (2.15 Å)